Canonical Allele Identifier: CA1107257346
Gene: MKLN1 HGNC NCBI

Linked Data

dbSNP Id: rs1234332935

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.131418750A>G , CM000669.2:g.131418750A>G GRCh38
NC_000007.13:g.131103509A>G , CM000669.1:g.131103509A>G GRCh37
NC_000007.12:g.130754049A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000352689.11:c.847+4040A>G MANE Select ENSP00000323527.6:n.847+4040A>G
ENST00000352689.10:c.847+4040A>G ENSP00000323527.6:n.847+4040A>G
ENST00000421797.6:c.571+4040A>G ENSP00000398094.2:n.571+4040A>G
ENST00000458153.5:c.*337+4040A>G ENSP00000407705.1:n.*337+4040A>G
ENST00000494785.5:n.864+4040A>G
NM_001145354.1:c.778+4040A>G NP_001138826.1:n.778+4040A>G
NM_013255.4:c.847+4040A>G NP_037387.2:n.847+4040A>G
XM_005250356.1:c.226+4040A>G XP_005250413.1:n.226+4040A>G
XM_006715993.1:c.847+4040A>G XP_006716056.1:n.847+4040A>G
XM_011516224.1:c.847+4040A>G XP_011514526.1:n.847+4040A>G
NM_001321316.1:c.226+4040A>G NP_001308245.1:n.226+4040A>G
XM_006715993.3:c.847+4040A>G XP_006716056.1:n.847+4040A>G
XM_011516224.3:c.847+4040A>G XP_011514526.1:n.847+4040A>G
XM_024446766.1:c.571+4040A>G XP_024302534.1:n.571+4040A>G
XM_024446767.1:c.571+4040A>G XP_024302535.1:n.571+4040A>G
NM_013255.5:c.847+4040A>G MANE Select NP_037387.2:n.847+4040A>G
NM_001145354.2:c.778+4040A>G NP_001138826.1:n.778+4040A>G
NM_001321316.2:c.226+4040A>G NP_001308245.1:n.226+4040A>G